Art
J-GLOBAL ID：200902157516750136
Reference number：00A0327245
Characteristic Features of the Genotype and Phenotype of Hereditary Spherocytosis in the Japanese Population.
日本人集団における遺伝性球状赤血球症の遺伝子型および表現型の特徴
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Material：
Volume：
71
Issue：
2
Page：
118-135
Publication year：
Feb. 2000
JST Material Number：
F0888A
ISSN：
0925-5710
CODEN：
IJHEEY
Document type：
Article
Article type：
原著論文
Country of issue：
Germany, Federal Republic of (DEU)
Language：
ENGLISH (EN)
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Semi thesaurus term：
Thesaurus term/Semi thesaurus term
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All keywords is available on JDreamIII(charged).
On J-GLOBAL, this item will be available after more than half a year after the record posted. In addtion, medical articles require to login to MyJ-GLOBAL.
JST classification (1)：
JST classification
Category name(code) classified by JST.
Hematologic diagnosis
Reference (57)：
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GALLAGHER, PG. Disorders of the erythrocyte membrane. Hematology of Infancy and Childhood. 1998, 544-664
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LUX, SE. Disorders of the red cell membrane. Blood, Principles and Practice of Hematology. 1995, 1701-1818
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LUX, SE. Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8. Nature. 1990, 345, 736-739
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EBER, SW. Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis. Nature Genet. 1996, 13, 214-218
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JAROLIM, P. Characterization of 13 novel band 3 gene defects in hereditary spherocytosis with band 3 deficiency. Blood. 1996, 88, 4366-4374
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